CHINDOC Pharma Services offers services to pharmaceutical, biotech and medical device companies in consultation on the Chinese pharmaceutical market, regulatory affairs and clinical trial services. We provide services in accordance with Good Clinical Practice in China and international guidelines such as ICH.
For Clinical Trial, We offer: |
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Feasibility studies
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Clinical project initiation including
submission of
applications to
the authority (SFDA) and Ethical Committees |
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Site recruitment and
set up of
financial agreements
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Monitoring
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Site
and project
management
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Investigators' meetings and GCP training of site staff
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Medical writing |
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Bioequivalence studies (Bridging studies for clinical trials related to
import registration) the complete package |
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Consultation about clinical trials in general in China |
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Translation of medical and clinical trial documents |
Services
